GLPBio

Diethylamino hydroxybenzoyl hexyl benzoate (DHHB)

Catalog No.: GC30590Purity:>98.00%
ジエチルアミノ ヒドロキシベンゾイル ヘキシル ベンゾエート (DHHB) は、光安定性の UV-A 吸収剤です。

製品は研究用途にのみ使用できます。人体には使用できません。患者への販売は行っておりません。


Diethylamino hydroxybenzoyl hexyl benzoate (DHHB)
Cas No.: 302776-68-7
1gIn Stock
$15.00
1
5gIn Stock
$25.00
1

引用文献 (Citations)

現在、この製品の引用文献はありません。以下はGlpBio製品を引用した代表的な文献です。
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    Nature
    641, 529–536 (2025)
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    Nature
    628, 630–638 (2024)
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    Nature
    632, 686–694 (2024)
  • Nature cover
    Nature
    618, 1017–1023 (2023)
  • Nature cover
    Nature
    610, 366–372 (2022)
  • Cell cover
    Cell
    187(9):2288-2304 (2024)
  • Cell cover
    Cell
    183(7):1867-1883 (2020)
  • Science cover
    Science
    388(6745) (2025)
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    Science
    387(6739) (2025)
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    Science
    387(6734) (2025)
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    Cell Research
    35, 97–116 (2025)
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    34, 683–706 (2024)
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    33, 273–287 (2023)
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    33, 546–561 (2023)
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    33, 904–922 (2023)
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    Cell Research
    31, 1291–1307 (2021)

製品説明 (Description)

Diethylamino hydroxybenzoyl hexyl benzoate (DHHB) is a substituted benzophenone-type organic UV filter. Diethylamino hydroxybenzoyl hexyl benzoate absorbs UVA radiation in the 320–400nm wavelength range through its conjugated aromatic structure and converts the absorbed light energy into heat, thereby protecting the skin from photodamage. Diethylamino hydroxybenzoyl hexyl benzoate can be used in sunscreens, day creams, and other cosmetic products to provide broad-spectrum UVA protection and is applied in anti-photoaging skincare products[1-4].

In vitro, 3T3 Balb/c fibroblasts were pre-treated for 1 hour with a combination containing Diethylamino hydroxybenzoyl hexyl benzoate (62.5μg/mL), octocrylene (75μg/mL), and octyl methoxycinnamate (100μg/mL), followed by UVA radiation (5J/cm²). The combination containing Diethylamino hydroxybenzoyl hexyl benzoate did not show phototoxic potential[5]. S. cerevisiae Ogg1 mutant strain (CD138) was pre-treated with Diethylamino hydroxybenzoyl hexyl benzoate (100μg/mL) for 6 hours, followed by stimulation with solar simulated light (SSL) (2.5–10kJ/m²). Diethylamino hydroxybenzoyl hexyl benzoate increased cell survival and protected yeast cells from the toxic effects of solar simulator radiation[6].

References:
[1] Fagervold SK, Rohée C, Lebaron P. Marine sediments microbes degrade a limited repertoire of organic UV filters. Environ Sci Pollut Res Int. 2025 Jul;32(33):19823-19835.
[2] Sobańska AW, Sobański AM, Brzezińska E. Organic Sunscreens-Biological Activity from an Enzymatic Perspective. Molecules. 2026 May 14;31(10):1656.
[3] Shamoto Y, Yagi M, Oguchi-Fujiyama N, et al. Photophysical properties of hexyl diethylaminohydroxybenzoylbenzoate (Uvinul A Plus), a UV-A absorber. Photochem Photobiol Sci. 2017 Sep 13;16(9):1449-1457.
[4] Ichikawa M, Shimokawa N, Makuta M, et al. Cytotoxicity, genotoxicity, and enzyme activity effects of UV filters and their chlorinated by-products in human lung epithelial cells (A549). Sci Total Environ. 2025 Sep 24;1002:180516.
[5] Kibwila DM, Simon A, de Abreu LCL, et al. New alternatives in photoprotection: Preparation and evaluation of lamellar silicate derivatives and their use as sunscreens. Int J Cosmet Sci. 2026 Feb;48(1):172-185.
[6] Murai M, Sakurada J, Seki K, et al. Apoptosis observed in BALB/3T3 cells having ingested Staphylococcus aureus. Microbiol Immunol. 1999;43(7):653-61.

実験プロトコル (Protocol)

Cell experiment [1]:

Cell lines

3T3 Balb/c fibroblasts (mouse fibroblast cell line)

Preparation Method

Fibroblasts were grown in two 96-well plates and preincubated with eight different concentrations of the combinations under study (C2: containing Diethylamino hydroxybenzoyl hexyl benzoate, octocrylene and octyl methoxycinnamate). After 1h incubation, one plate was subjected to 5J/cm² of UVA radiation (+UV plate) and the other was kept in a dark box (-UV plate). Cell viability was assessed by determining the uptake of neutral red dye.

Reaction Conditions

62.5μg/mL; 1h preincubation

Applications

Combinations containing Diethylamino hydroxybenzoyl hexyl benzoate did not show a phototoxic potential in the 3T3 Neutral Red Uptake Phototoxicity Test.

References:
[1] Kawakami CM, Máximo LN, Fontanezi BB, et al. Diethylamino hydroxybenzoyl hexyl benzoate (DHHB) as additive to the UV filter avobenzone in cosmetic sunscreen formulations - Evaluation of the photochemical behavior and photostabilizing effect. Eur J Pharm Sci. 2017 Mar 1;99:299-309.

製品資料 (Product Documents)

Purity:>98.00%Appearance:A solid

化学的性質 (Chemical Properties)

CAS番号
302776-68-7
SMILES
O=C(OCCCCCC)C1=CC=CC=C1C(C2=CC=C(N(CC)CC)C=C2O)=O
分子式
C24H31NO4
分子量
397.51
溶解性
DMSO : ≥ 50 mg/mL (125.78 mM)
保存条件
Store at -20°C, protect from light
一般的な注意事項
製品の溶解性データに基づいて適切な溶媒を選択してください。調製後は、凍結融解の繰り返しを避けるため、ストック溶液を小分けしてください。
ストック溶液は、-80°Cで保存する場合は6か月以内、-20°Cで保存する場合は1か月以内に使用してください。
溶解性を高めるには、チューブを37°Cに温め、適切な時間超音波処理してください。
配送条件
評価用サンプルは保冷剤とともに発送します。その他の容量は室温で発送し、ご要望に応じて保冷剤を同梱します。

計算ツール (Calculators)モル濃度 / 希釈 / 分子量 / 単位変換 / in vivo製剤 / 溶解度

g/mol

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